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The non-NMDA glutamate receptor antagonist GYKI 52466 counteracts locomotor stimulation and anticataleptic activity induced by the NMDA antagonist dizocilpine

机译:非NmDa谷氨酸受体拮抗剂GYKI 52466抵消由NmDa拮抗剂地佐环平诱导的运动刺激和抗癫痫活性

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摘要

The effects of the non-NMDA glutamate receptor antagonist GYKI 52466 (2.4 and 4.8 mg/kg, i.p.) on spontaneous locomotor activity and haloperidol-induced catalepsy (0.5 mg/kg, i.p.) were assessed in naive rats and in rats pretreated with the NMDA antagonist dizocilpine (0.08 mg/kg, i.p.). GYKI 52466 given alone did not alter locomotor activity and haloperidol-induced catalepsy, but significantly antagonized the dizocilpine-induced locomotor stimulation and counteracted the anti-cataleptic effects of dizocilpine on haloperidol-induced catalepsy. Thus blockade of non-NMDA glutamate receptors antagonized the behavioural stimulant effects of a NMDA receptor blockade.
机译:在幼稚大鼠和接受过NMDA预处理的大鼠中,评估了非NMDA谷氨酸受体拮抗剂GYKI 52466(2.4和4.8 mg / kg,ip)对自发运动活性和氟哌啶醇诱导的僵直(0.5 mg / kg,ip)的影响。 NMDA拮抗剂地佐西平(0.08 mg / kg,ip)。单独服用的GYKI 52466不会改变运动活性和氟哌啶醇诱导的僵直,但明显拮抗地佐西平诱导的运动刺激,并抵消了地佐西平对氟哌啶醇诱导的僵直的抗镇痛作用。因此,非NMDA谷氨酸受体的阻断拮抗了NMDA受体阻断的行为刺激作用。

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